Canonical Allele Identifier: CA418539878

Gene: ACADM

Linked Data

• MyVariant Identifiers: chr1:g.76205679A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.75739994A>G , CM000663.2:g.75739994A>G	GRCh38
NC_000001.10:g.76205679A>G , CM000663.1:g.76205679A>G	GRCh37
NC_000001.9:g.75978267A>G	NCBI36
NG_007045.2:g.20637A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370841.9:c.483A>G MANE Select	ENSP00000359878.5:p.Thr161=
ENST00000473018.3:n.2607A>G
ENST00000541113.6:c.483A>G	ENSP00000442324.2:p.Thr161=
ENST00000679509.1:n.1445A>G
ENST00000679530.1:c.*251A>G	ENSP00000506454.1:n.*251A>G
ENST00000679615.1:n.2607A>G
ENST00000679687.1:c.45A>G	ENSP00000506598.1:p.Thr15=
ENST00000679704.1:c.*249A>G	ENSP00000505117.1:n.*249A>G
ENST00000679709.1:c.*446A>G	ENSP00000506623.1:n.*446A>G
ENST00000679804.1:n.222A>G
ENST00000679976.1:c.*67A>G	ENSP00000505565.1:n.*67A>G
ENST00000680166.1:n.3772A>G
ENST00000680517.1:c.301A>G	ENSP00000505803.1:p.Arg101Gly
ENST00000680582.1:n.1445A>G
ENST00000680613.1:c.483A>G	ENSP00000506114.1:p.Thr161=
ENST00000680662.1:c.*397A>G	ENSP00000505080.1:n.*397A>G
ENST00000680691.1:c.*146A>G	ENSP00000506487.1:n.*146A>G
ENST00000680694.1:c.*71A>G	ENSP00000505658.1:n.*71A>G
ENST00000680743.1:c.*150A>G	ENSP00000505073.1:n.*150A>G
ENST00000680749.1:c.483A>G	ENSP00000505122.1:p.Thr161=
ENST00000680798.1:c.*67A>G	ENSP00000505670.1:n.*67A>G
ENST00000680805.1:c.483A>G	ENSP00000505447.1:p.Thr161=
ENST00000680844.1:c.*267A>G	ENSP00000506541.1:n.*267A>G
ENST00000680948.1:c.*350A>G	ENSP00000505441.1:n.*350A>G
ENST00000680964.1:c.483A>G	ENSP00000505961.1:p.Thr161=
ENST00000681037.1:c.483A>G	ENSP00000506025.1:p.Thr161=
ENST00000681063.1:c.483A>G	ENSP00000506616.1:p.Thr161=
ENST00000681209.1:c.*247A>G	ENSP00000505877.1:n.*247A>G
ENST00000681278.1:n.840A>G
ENST00000681289.1:n.840A>G
ENST00000681361.1:c.*150A>G	ENSP00000506679.1:n.*150A>G
ENST00000681430.1:c.483A>G	ENSP00000506301.1:p.Thr161=
ENST00000681446.1:c.*65A>G	ENSP00000506244.1:n.*65A>G
ENST00000681450.1:c.*154A>G	ENSP00000505660.1:n.*154A>G
ENST00000681548.1:c.*69A>G	ENSP00000505275.1:n.*69A>G
ENST00000681616.1:c.*251A>G	ENSP00000505111.1:n.*251A>G
ENST00000681621.1:c.*67A>G	ENSP00000505770.1:n.*67A>G
ENST00000681680.1:n.2607A>G
ENST00000681720.1:c.*55-5812A>G	ENSP00000505438.1:n.*55-5812A>G
ENST00000681730.1:n.705A>G
ENST00000681790.1:c.225A>G	ENSP00000505130.1:p.Thr75=
ENST00000681837.1:n.1099A>G
ENST00000681913.1:n.2607A>G
ENST00000681916.1:c.*251A>G	ENSP00000506477.1:n.*251A>G
ENST00000681930.1:n.2607A>G
ENST00000370834.9:c.582A>G	ENSP00000359871.5:p.Thr194=
ENST00000370841.8:c.483A>G	ENSP00000359878.4:p.Thr161=
ENST00000420607.6:c.495A>G	ENSP00000409612.2:p.Thr165=
ENST00000525808.5:c.*69A>G	ENSP00000434823.1:n.*69A>G
ENST00000526129.5:c.*267A>G	ENSP00000434092.1:n.*267A>G
ENST00000526196.5:c.*251A>G	ENSP00000431953.1:n.*251A>G
ENST00000526930.1:n.256A>G
ENST00000529059.5:n.392A>G
ENST00000530953.6:c.133A>G	ENSP00000431372.1:p.Arg45Gly
ENST00000532509.5:c.*247A>G	ENSP00000432522.1:n.*247A>G
ENST00000534334.5:c.*67A>G	ENSP00000435584.1:n.*67A>G
ENST00000541113.5:c.375A>G	ENSP00000442324.1:p.Thr125=
NM_000016.5:c.483A>G	NP_000007.1:p.Thr161=
NM_001127328.2:c.495A>G	NP_001120800.1:p.Thr165=
NM_001286042.1:c.375A>G	NP_001272971.1:p.Thr125=
NM_001286043.1:c.582A>G	NP_001272972.1:p.Thr194=
NM_001286044.1:c.-85A>G	NP_001272973.1:n.-85A>G
NM_000016.6:c.483A>G MANE Select	NP_000007.1:p.Thr161=
NM_001127328.3:c.495A>G	NP_001120800.1:p.Thr165=
NM_001286042.2:c.375A>G	NP_001272971.1:p.Thr125=
NM_001286043.2:c.582A>G	NP_001272972.1:p.Thr194=
NM_001286044.2:c.-85A>G	NP_001272973.1:n.-85A>G